ACADL antibody

Catalog No. ABIN2458052

Product Details anti-ACADL Antibody

Target: ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ACADL antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ACADL.

Application Details

Application Notes: ACADL antibody can be used for detection of ACADL by ELISA at 1:312500. ACADL antibody can be used for detection of ACADL by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handling Advice: As with any antibody avoid repeat freeze-thaw cycles.

Storage: 4 °C/-20 °C

Storage Comment: For short periods of storage (days) store at 4 °C. For longer periods of storage, store ACADL antibody at -20 °C.

Target Details for ACADL

Target: ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

Alternative Name: ACADL (ACADL Products)

Synonyms: zgc:55656 antibody, ACAD4 antibody, LCAD antibody, ACOADA antibody, AA960361 antibody, AU018452 antibody, C79855 antibody, acyl-CoA dehydrogenase long chain antibody, acyl-CoA dehydrogenase, long chain antibody, acyl-CoA dehydrogenase, long chain L homeolog antibody, acyl-Coenzyme A dehydrogenase, long-chain antibody, acadl antibody, ACADL antibody, Acadl antibody, acadl.L antibody

Background: ACADL belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.

Molecular Weight: 44 kDa

Gene ID: 33

NCBI Accession: NP_001599

UniProt: P28330

Pathways: Monocarboxylic Acid Catabolic Process